Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience - 1 Jan 2000

Bartlett Christopher W, Gharani Neda, Millonig James H, Brzustowicz Linda M

Abstract excerpt

Autism is a particularly complex disorder when considered from virtually any methodological framework, including the perspective of human genetics. We first present a review of the genetic analysis principles relevant for discussing autism genetics research. From this body of work we highlight re...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autistic Disorder
Share to Cell Adhesion Molecules, Neuronal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Genetic Techniques

Share to Membrane Transport Proteins

Share to Reelin Protein

Share to Serine Endopeptidases

Share to Serotonin Plasma Membrane Transport Proteins

Source

Identifiers

PMID: 15749247
DOI: 10.1016/j.ijdevneu.2004.10.004

Genes

RELN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15749247-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.PMID 15749247Read ↗

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.Semantic proximity Read ↗

Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.Semantic proximity Read ↗

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.Semantic proximity Read ↗

Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.Semantic proximity Read ↗

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.Semantic proximity Read ↗

Epigenetic factors and autism spectrum disorders.Semantic proximity Read ↗

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.Semantic proximity Read ↗

Analysis of the RELN gene as a genetic risk factor for autism.Semantic proximity Read ↗

Heterogeneous association between engrailed-2 and autism in the CPEA network.Semantic proximity Read ↗

Analysis of reelin as a candidate gene for autism.Semantic proximity Read ↗

Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum.Semantic proximity Read ↗

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.